Ueli Suter
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Glycolytic oligodendrocytes maintain myelin and long-term axonal integrity
U Fünfschilling, LM Supplie, D Mahad, S Boretius, AS Saab, J Edgar, ...
Nature 485 (7399), 517-521, 2012
The gene for the peripheral myelin protein PMP–22 is a candidate for Charcot–Marie–Tooth disease type 1A
PI Patel, BB Roa, AA Welcher, R Schoener-Scott, BJ Trask, L Pentao, ...
Nature genetics 1 (3), 159-165, 1992
CNS-resident glial progenitor/stem cells produce Schwann cells as well as oligodendrocytes during repair of CNS demyelination
M Zawadzka, LE Rivers, SPJ Fancy, C Zhao, R Tripathi, F Jamen, ...
Cell stem cell 6 (6), 578-590, 2010
Instructive role of Wnt/ß-catenin in sensory fate specification in neural crest stem cells
HY Lee, M Kléber, L Hari, V Brault, U Suter, MM Taketo, R Kemler, ...
Science 303 (5660), 1020-1023, 2004
Trembler mouse carries a point mutation in a myelin gene
U Suter, AA Welcher, T Özcelik, GJ Snipes, B Kosaras, U Francke, ...
Nature 356 (6366), 241-244, 1992
Schwann cell precursors from nerve innervation are a cellular origin of melanocytes in skin
I Adameyko, F Lallemend, JB Aquino, JA Pereira, P Topilko, T Müller, ...
Cell 139 (2), 366-379, 2009
Characterization of a novel peripheral nervous system myelin protein (PMP-22/SR13)
GJ Snipes, U Suter, AA Welcher, EM Shooter
The Journal of cell biology 117 (1), 225-238, 1992
Disease mechanisms in inherited neuropathies
U Suter, SS Scherer
Nature reviews neuroscience 4 (9), 714-726, 2003
Ganglioside-induced differentiation associated protein 1 is a regulator of the mitochondrial network: new implications for Charcot-Marie-Tooth disease
A Niemann, M Ruegg, V La Padula, A Schenone, U Suter
The Journal of cell biology 170 (7), 1067-1078, 2005
Charcot-Marie-Tooth Disease Type 1A--Association with a Spontaneous Point Mutation in the PMP22 Gene
BB Roa, CA Garcia, U Suter, DA Kulpa, CA Wise, J Mueller, AA Welcher, ...
New England Journal of Medicine 329 (2), 96-101, 1993
Hypermyelination and demyelinating peripheral neuropathy in Pmp22-deficient mice
K Adlkofer, R Martini, A Aguzzi, J Zielasek, KV Toyka, U Suter
Nature genetics 11 (3), 274-280, 1995
Molecular cloning and characterization of N-syndecan, a novel transmembrane heparan sulfate proteoglycan
DJ Carey, DM Evans, RC Stahl, VK Asundi, KJ Conner, P Garbes, ...
The Journal of cell biology 117 (1), 191-201, 1992
A transgenic rat model of Charcot-Marie-Tooth disease
M Sereda, I Griffiths, A Pühlhofer, H Stewart, MJ Rossner, F Zimmermann, ...
Neuron 16 (5), 1049-1060, 1996
Lineage-specific requirements of β-catenin in neural crest development
L Hari, V Brault, M Kléber, HY Lee, F Ille, R Leimeroth, C Paratore, ...
The Journal of cell biology 159 (5), 867-880, 2002
Metabolic control of adult neural stem cell activity by Fasn-dependent lipogenesis
M Knobloch, SMG Braun, L Zurkirchen, C Von Schoultz, N Zamboni, ...
Nature 493 (7431), 226-230, 2013
Survival and glial fate acquisition of neural crest cells are regulated by an interplay between the transcription factor Sox10 and extrinsic combinatorial signaling
C Paratore, DE Goerich, U Suter, M Wegner, L Sommer
Development 128 (20), 3949-3961, 2001
Jagged1-dependent Notch signaling is dispensable for hematopoietic stem cell self-renewal and differentiation
SJC Mancini, N Mantei, A Dumortier, U Suter, HR MacDonald, F Radtke
Blood 105 (6), 2340-2342, 2005
Therapeutic administration of progesterone antagonist in a model of Charcot-Marie-Tooth disease (CMT-1A)
MW Sereda, GM zu Hörste, U Suter, N Uzma, KA Nave
Nature medicine 9 (12), 1533-1537, 2003
Neural crest–derived cells with stem cell features can be traced back to multiple lineages in the adult skin
CE Wong, C Paratore, MT Dours-Zimmermann, A Rochat, T Pietri, U Suter, ...
The Journal of cell biology 175 (6), 1005-1015, 2006
Structural abnormalities and deficient maintenance of peripheral nerve myelin in mice lacking the gap junction protein connexin 32
P Anzini, DHH Neuberg, M Schachner, E Nelles, K Willecke, J Zielasek, ...
Journal of Neuroscience 17 (12), 4545-4551, 1997
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